Zobrazeno 1 - 10
of 90
pro vyhledávání: '"J L, Huret"'
Autor:
J. L. Huret
Publikováno v:
Atlas of Genetics and Cytogenetics in Oncology and Haematology.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::b4140abac226657b18b9762813b03d22
https://doi.org/10.4267/2042/70617
https://doi.org/10.4267/2042/70617
Publikováno v:
Leukemialymphoma. 4(1)
Twenty-four patients with Philadelphia positive (Ph +) chronic myelogenous leukemia including 12 who were previously untreated, received recombinant interferon alpha-2a (IFN) (5 × 10(6) U/m(2)/d) and hydroxyurea (HU) (50 mg/kg/d) at the induction ph
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::fef146ca38c282fc9794ac1ed679324c
https://pubmed.ncbi.nlm.nih.gov/27462717
https://pubmed.ncbi.nlm.nih.gov/27462717
Autor:
André Brizard, P. Babin, Joseph Tanzer, J. L. Huret, Laura Demeure, Elisabeth Benz-lemoine, Marie-Cecile Desmarest
Publikováno v:
Leukemialymphoma. 4(3)
We report two cases of t(12;13)(p13;q12). One was found in a lymphoid disorder, as previously described, while the second was observed in a myeloproliferative syndrome with hypereosinophilia. As t(12;13) has already been described in association with
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::cbbab5d91354ac5d2873b3e8885593e4
https://pubmed.ncbi.nlm.nih.gov/27458675
https://pubmed.ncbi.nlm.nih.gov/27458675
Publikováno v:
Clinical Genetics. 28:541-545
Analysis of the karyotype of an azoospermic 27-year-old man, without any dysmorphism, showed the presence of a ring chromosome 21.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::4c717171d96027d188ca63c0e72466cb
https://doi.org/10.1111/j.1399-0004.1985.tb00423.x
https://doi.org/10.1111/j.1399-0004.1985.tb00423.x
Autor:
C. Léonard, J. L. Huret
Publikováno v:
Clinical Genetics. 34:276-278
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::7c1407e560403d63c46ecc7187c08f68
https://doi.org/10.1111/j.1399-0004.1988.tb02876.x
https://doi.org/10.1111/j.1399-0004.1988.tb02876.x
Publikováno v:
Nucleic Acids Research. 31:272-274
The 'Atlas of Genetics and Cytogenetics in Oncology and Haematology' (http://www.infobiogen.fr/services/chromcancer) contains concise and updated cards on genes involved in cancer, cytogenetics and clinical entities in oncology, and cancer-prone dise
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::eeb7079e08598f9eed17dda456c8b10c
https://doi.org/10.1093/nar/gkg126
https://doi.org/10.1093/nar/gkg126
Publikováno v:
Atlas of Genetics and Cytogenetics in Oncology and Haematology.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::5497ae2e5177fafbb41a87e9411ec5df
https://doi.org/10.4267/2042/37658
https://doi.org/10.4267/2042/37658
Publikováno v:
Leukemia Research. 16:537-540
We report on four cases of trisomy 14 as the sole anomaly. Three cases were myelodysplastic syndromes and one was a non-Hodgkin's lymphoma. This anomaly is mainly in myeloid disorders and still remains to be well documented. On the other hand, we sho
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::cb989d8d95c2a218cdd3fbfb42d0dc83
https://doi.org/10.1016/0145-2126(92)90181-6
https://doi.org/10.1016/0145-2126(92)90181-6
Autor:
J. L. Huret, Michèle Schoënwald, François Guilhot, P. Babin, André Brizard, Sylvain Briault, Joseph Tanzer
Publikováno v:
Cancer Genetics and Cytogenetics. 45:125-129
We report two cases of t(8;9) with probable breakpoints in 8q12 and 9p21 in malignant lymphoma. In a review of the literature, we found two cases of acute lymphocytic leukemia and one case of malignant lymphoma which probably share the same breakpoin
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::a4845151f030a7da59da48ebd596d55d
https://doi.org/10.1016/0165-4608(90)90075-l
https://doi.org/10.1016/0165-4608(90)90075-l
Autor:
Hervé Tilly, Roger A. Warnke, Christian Bastard, J. Hemet, Nicole Dastugue, Ruth Rimokh, J-P. Vannier, U. Kristoffersson, J-P. Magaud, C. Nezelof, J-L. Huret
Publikováno v:
British Journal of Haematology. 74:161-168
Summary A chromosomal translocation involving a breakpoint on the long arm of chromosome 5 at position q35 has been reported previously in 17 cases of neoplasia. In 14 of these cases the translocation involves exchange of material between chromosome
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::c31f53ceeffa13ef0b75aa5e2bfdda72
https://doi.org/10.1111/j.1365-2141.1990.tb02560.x
https://doi.org/10.1111/j.1365-2141.1990.tb02560.x